Drive regulatory content strategies as a Senior Medical Writer with Amaris Consulting in a hybrid work model. Lead the formulation of key documentation for global submissions, ensuring compliance and high standards. In this permanent role, you will manage complex regulatory documentation while guiding submission strategies for pharmaceuticals and medical devices.

Your expertise will help primary stakeholders prepare clinical dossiers and safety documents, maintaining alignment with the overall project timelines. Collaboration with cross-functional teams will be crucial for timely delivery and integration of core content messages throughout regulatory submissions. Key Responsibilities:
Lead regulatory content strategy development for global authorities




Manage preparation of clinical dossiers and safety documentation
Develop content plans aligning with project schedules
Review regulatory documents for accuracy and compliance
Maintain inspection readiness for all documentation Requirements:
Bachelor’s in Life Sciences or related field
Minimum 5 years in regulatory or medical writing
Solid knowledge of global regulatory processes
Proven experience in leading complex documentation
Proficient in Google Workspace and Microsoft Office Utilize your expertise to elevate regulatory standards and support submission success at Amaris Consulting.

📌 Senior Medical Writer At Amaris Consulting Mississauga
🏢 AMARIS GROUP
📍 Mississauga